Study of Atorvastatin/Fenofibrate (LCP-AtorFen) Combination Therapy in Dyslipidemia
NCT00504829 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 220
Last updated 2020-02-17
Summary
The current study is designed to test the efficacy, safety and tolerability of LCP-AtorFen, a combination of atorvastatin and fenofibrate.
Conditions
Interventions
- DRUG
-
LCP-AtorFen
40mg atorvastatin combined with 100mg fenofibrate in a tablet for once daily treatment of dyslipidemia and mixed dyslipidemia
- DRUG
-
dyslipidemia and mixed dyslipidemia
- DRUG
-
fenofibrate
dyslipidemia and mixed dyslipidemia
Sponsors & Collaborators
-
Veloxis Pharmaceuticals
lead INDUSTRY
Principal Investigators
-
Jeff Geohas, MD · Radiant Research
-
Dennis McCluskey, MD · Radiant Research
-
Harry Geisberg, MD · Radiant Research
-
Chivers Woodruff, Jr, MD · Radiant Research
-
Michael Noss, MD · Radiant Research
-
Michele Reynolds, MD · Radiant Research
-
James Zavoral, MD · Radiant Research
-
Randall Severance, MD · Radiant Research
-
Stephen Halpern, MD · Radiant Research
-
Linda Murray, MD · Radiant Research
-
Wayne Larson, MD · Radiant Research
-
Timothy Howards, MD · Medical Affiliated Research Center, Inc.
-
Cynthia Strout, MD · Coastal Carolina Research Center
-
Mark Kipnes, MD · Diabetes and Glandular Research Center, Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-07-31
- Primary Completion
- 2008-02-29
- Completion
- 2008-07-31
Countries
- United States
Study Locations
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